Clinical trials: Reaching
Stroke
Reaching Training Based on Robotic Hybrid Assistance for Stroke Patients ( RETRAINER-S2 )
Stroke is the third most common cause of death and the main cause of acquired adult disability in high-income countries. The most common deficit after stroke is motor impairment of the contralateral arm, with more than 80% of…
- Trial name
- RETRAINER-S2 (NCT03199833)
- Testing
- RETRAINER-S2, Conventional therapy
- Where
- 2 sites in Germany, Italy
- Volunteers
- 68 people
- Sponsor
- Dr. Franco Molteni
HIV
Reaching the Last 20% (the Pamoja Kwa Afya Study)
This cluster randomized controlled trial will test whether the provision of multiple oral fluid-based HIV self-test kits to women who sell sex (WSS) to secondarily distribute to their male partners who purchase sex can promote…
- Trial name
- NCT05882916
- Testing
- HIV self-testing, Behavioral economic 'nudges'
- Where
- Kenya
- Volunteers
- 5,000 people, healthy volunteers welcome
- Sponsor
- Sue Napierala
Reproductive Health, Sexual Health
Estimating the Impact of Sexuality Education and Mobile Health Services on Reproductive Health and Empowerment Among Adolescents in Sierra Leone for the Family Planning Impact Lab
The goal of this randomized controlled trial is to learn if comprehensive sexuality education (CSE) and access to mobile sexual and reproductive health (SRH) services in secondary schools can improve short- and long-term health…
- Conditions
- Reproductive Health, Sexual Health, Contraception Behavior, Pregnancy (Unwanted)
- Trial name
- REACH (NCT07860723)
- Testing
- Comprehensive Sexuality Education, Mobile SRH services
- Where
- Sierra Leone
- Volunteers
- 5,300 people, healthy volunteers welcome
- Sponsor
- Guttmacher Institute
Cervical Cancer, Cervical Intraepithelial Neoplasia
Dry Run of the ScreenUrSelf Trial
The proposed study is the Dry Run preceding the ScreenUrSelf trial.
- Conditions
- Cervical Cancer, Cervical Intraepithelial Neoplasia, Human Papilloma Virus, HPV-Related Cervical Carcinoma
- Trial name
- NCT05996796
- Testing
- Colli-Pee Small Volumes, Evalyn Brush
- Where
- Belgium
- Volunteers
- 38 people, healthy volunteers welcome
- Sponsor
- Universiteit Antwerpen
Lung Nodule
Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic Needle Aspiration
This study will evaluate which procedure is the best for patients referred for biopsy of a lung nodule (growth in the lung) meeting the size and location requirements of the protocol.
- Trial name
- VERITAS (NCT04250194)
- Testing
- CT-Guided Biopsy, Navigation bronchoscopy
- Where
- 7 sites in United States
- Volunteers
- 288 people
- Sponsor
- Vanderbilt-Ingram Cancer Center
Diabetes Mellitus Type 1
Comparing Continuous Subcutaneous Insulin Infusion With Multiple Daily Injections to Reach HbA1c Targets in Children and Adolescents With Type 1 Diabetes
This study is to compare metabolic control, treatment satisfaction, and quality of life during continuous subcutaneous insulin infusion (CSII ) therapy with a new insulin pump system with multiple daily injections (MDI) therapy.
- Trial name
- Insight Kids (NCT02403375)
- Testing
- Accu-Chek Insight Pump System
- Where
- 9 sites in Austria, Germany and 1 more
- Volunteers
- 43 people
- Sponsor
- Hoffmann-La Roche
Heavy Menstrual Bleeding, Uterine Fibroids
A Study to Assess Patient-Reported Quality of Life and Effectiveness on Control of Bleeding in Adult Participants With Heavy Menstrual Bleeding Due to Uterine Fibroids Taking Oral Oriahnn Capsules
Uterine Fibroids (UF) are noncancerous (benign) tumors that commonly occur in up to 80% of women of reproductive age. Symptoms can include heavy menstrual bleeding (HMB), low back pain, urinary frequency and urgency…
- Trial name
- REACH (NCT05026502)
- Where
- United States
- Volunteers
- 23 people
- Sponsor
- AbbVie
Hypertension
"Real-world Assessment of BP Control in Patients With Hypertension by the Netrod RDN System" - REACH-RDN
This study is an observational one, collecting real-world data generated in routine clinical treatment. The Netrod-RDN renal artery radiofrequency ablation system (including the renal artery radiofrequency ablation device and the…
- Trial name
- NCT07273877
- Testing
- Percutaneous nephrolysis combined with sympathetic nerve ablation (RDN) procedure
- Where
- China
- Volunteers
- 1,000 people
- Sponsor
- Shanghai Golden Leaf MedTec Co. Ltd
Anxiety, Depression
Virtual Intervention for Behavioral Health in Emerging Adults; "VIBE in the Parks"
The goal of this study is first to develop and adapt a digital low-intensity treatment, "VIBE in the Parks", for adolescents and young adults (AYA) who visit programming at the Chicago Park District.
- Trial name
- VIBE (NCT07539636)
- Testing
- "VIBE in the Parks", Digital Control
- Volunteers
- 268 people
- Sponsor
- University of Illinois Chicago
Stroke, Spastic Hemiplegia
The Effects of Neurorehabilitation Approaches Involving Different Upper Extremity Reactive Trainings in Stroke Patients
The goal of this clinical trial is to investigate the effectiveness of upper extremity training, which is expected for 5 seconds on the target during reaching forward, and to compare the effectiveness of neurorehabilitation…
- Trial name
- NCT06086314
- Testing
- reactive exercise training with ''FitPodz Light Trainer'' device in addition to a neurorehabilitation program, reactive exercise training with co-contraction with ''FitPodz Light Trainer'' device in addition to a neurorehabilitation program., neurorehabilitation program with functional reaching training without device.
- Where
- 2 sites in Turkey (Türkiye)
- Volunteers
- 30 people
- Sponsor
- Pamukkale University
Depression, Anxiety, Post Traumatic Stress Disorder
Adaptation and Evaluation of the KEEP Model
This study capitalizes on an opportunity to formally evaluate local adaptations of "Keeping Foster and Kinship Parents Supported and Trained" (KEEP), an evidence-based foster parent intervention, to reduce mental health…
- Conditions
- Depression, Anxiety, Post Traumatic Stress Disorder, Suicide and Self-harm, Externalizing Behavior
- Trial name
- NCT05816421
- Testing
- KEEP, Non-Affinity KEEP
- Where
- United States
- Volunteers
- 283 people
- Sponsor
- Oregon Social Learning Center
Post-partum Depression
Preventing Postpartum Depression in Prenatal Care
This is randomized control trial of a brief intervention called Bellevue ROSE (Reach Out Stay Strong Essentials). Bellevue ROSE is a manualized and highly structured interpersonal intervention that provides women with…
- Trial name
- NCT02741206
- Testing
- Bellevue ROSE Intervention, Psycho-education session and usual, Standard of care Control, One Psycho-education session and usual, standard of care Control
- Where
- United States
- Sponsor
- NYU Langone Health
Extra Uterine Growth Restriction, Premature Infant Disease
Does Starting Feeds on the First Day of Life Help Premature Infants Reach Full Volume Feeds Sooner?
Feeding advancements in ELBW infants have evolved over decades. The fear of causing mortality and morbidity, notably NEC, have made providers cautious when advancing feeds.
- Conditions
- Extra Uterine Growth Restriction, Premature Infant Disease, VLBW - Very Low Birth Weight Infant
- Trial name
- NCT06731439
- Testing
- Starting feeds within 6 hours of life, Standard feeding protocol
- Where
- United States
- Volunteers
- 248 people
- Sponsor
- University of Tennessee
Group B Streptococcus
Oral Penicillin and Penicillin Levels in Venous Umbilical Cord Blood
Pregnant,laboring women will receive 2 grams of oral penicillin V before delivery. At the time of delivery of the infant, umbilical vein cord blood will be obtained from the umbilical cord.
- Trial name
- NCT00823433
- Testing
- oral penicillin V
- Where
- United States
- Volunteers
- 25 people, healthy volunteers welcome
- Sponsor
- Corewell Health East
Chronic Hepatitis B
Performance of Novel Simplified Score for Chronic Hepatitis B Treatment Eligibility in Thailand
International and national guideline for chronic hepatitis B (HBV) infection treatment recommend initiated antiviral in high HBV viral loads patients with significant liver inflammation and significant liver fibrosis.
- Trial name
- NCT05295914
- Testing
- TREAT-B score
- Where
- Thailand
- Volunteers
- 600 people
- Sponsor
- Mahidol University
Sleep Apnea
Reaching for Equity in Sleep Apnea Treatment (REST) Study
This study will test a brief telephonic health coaching intervention to improve adherence to positive airway pressure therapy for treatment of obstructive sleep apnea.
- Trial name
- REST pilot (NCT04209985)
- Testing
- Health coaching
- Where
- United States
- Volunteers
- 27 people, healthy volunteers welcome
- Sponsor
- University of California, San Francisco
Colorectal Cancer
Promoting CRC Screening in an Urban Minority Population
The purpose of this study (Healthy Colon Project II) is to evaluate different educational approaches for increasing rates of colorectal cancer (CRC) screening in a hard-to-reach urban minority population with health insurance.
- Trial name
- NCT02392143
- Testing
- Printed Education Material, Academic Detailing, Academic Detailing+Telephone Education
- Volunteers
- 564 people, healthy volunteers welcome
- Sponsor
- Teachers College, Columbia University
Aspergillosis Invasive, Fungal Infection
CYP2C19 Genotype-Specific Dosing Plus TDM on Reaching Therapeutic Voriconazole Blood Levels
Invasive aspergillosis is a fungal infection which left untreated, is a significant cause of morbidity and mortality. Immunocompromised patient populations such as solid organ transplant and malignant hematology patients are…
- Trial name
- NCT03731169
- Testing
- Voriconazole genotype-specific dosing, Standard of Care
- Where
- 2 sites in Canada
- Volunteers
- 30 people
- Sponsor
- University Health Network, Toronto
Gout
Gout Self-Monitoring Aiming to Reach Target
This study evaluates whether a supported self-management approach to gout is able to achieve target levels of serum urate, and better control of gout flares.
- Trial name
- Gout-SMART (NCT03274063)
- Testing
- Supported self-management, Usual care
- Where
- United Kingdom
- Volunteers
- 60 people
- Sponsor
- University of Edinburgh
Diabetes, Diabetes Mellitus, Type 2
INITIATE Plus (INITiation of Insulin to Reach A1c TargEt) Study
This trial is conducted in the United States of America (USA). The purpose of this study is to compare the effectiveness and safety of a biphasic insulin aspart standard titration regimen when coupled with dietary intervention to…
- Trial name
- INITIATE plus (NCT00101751)
- Testing
- biphasic insulin aspart, dietary regimen
- Where
- United States
- Volunteers
- 4,877 people
- Sponsor
- Novo Nordisk A/S